FDA recall record

CHINA-GEL CHINA_GEL recall — FDA D-0788-2021

CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.

Class IIclassification
D-0788-2021official record ID
Sep 8, 2021report date

Recall record at a glance

Official recordD-0788-2021
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmChina Gel Inc.
Report dateSep 8, 2021
Recall initiation dateMar 10, 2021
Quantity92,472 each
LocationArlington Heights, IL, United States

Official product description

CHINA_GEL (Camphor 3.00%, Menthol 5.00%) A TOPICAL PAIN RELIEVER, packaged as a) 2 OZ (56.8g) tube, NDC 76305-300-13; b) 4 OZ (113.5g) jar, UPC 6 87806 10004 2, NDC 76305-300-02; c) 6 OZ (170 g) tube, UPC 6 87806 10006 2, NDC 76305-300-03; d) 8 OZ (226.8g) jar, UPC 6 87806 10008 2, NDC 76305-300-04; e) 16 OZ (453.6g), Bottle w/ Pump, UPC 6 87806 10016 7, NDC 76305-300-03; f) 128 OZ (3.78L) Gallon, UPC 6 87806 10128 7, NDC 76305-300-06; Distributed by: CHINA-GEL LLC, Arlington Heights, IL 60005,

Why the product was recalled

CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.

Distribution information

Distributed Nationwide in the USA as well as Australia, Canada, France, Germany, Ireland, Norway, Turks & Caicos, Republic of Maldives, Russia, Singapore, Switzerland, United Kingdom

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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Related recall records

Other records from the same recalling company are shown first when available.

DrugSep 8, 2021

CHINA-GEL WHITE recall — FDA D-0789-2021

CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.

Class IIFDA: OngoingChina Gel Inc.
DrugSep 8, 2021

aulief recall — FDA D-0790-2021

CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.

Class IIFDA: OngoingChina Gel Inc.